meddevicedb.com FDA Device Reference

MONARCH SPINE SYSTEM

K024348 Class II Special
Decision Date
2003-01-28
Sponsor / Applicant
Depuyacromed

Technical Specification

510(k) Submission ID K024348
Product Code MNH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2003-01-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MONARCH SPINE SYSTEM received FDA 510(k) clearance under submission number K024348, sponsored by Depuyacromed. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2003-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code MNH and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.